HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2389269Erstellt: 26. Oktober 2026
Triethylamine → Tert-butyl 4-(2-cyano-1-benzofuran-5-yl)piperazine-1-carboxylate
https://huagongshe.com/reaction/2389269
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Trifluoroacetic anhydride | HCID 9845 | — |
| Edukt | Tert-butyl 4-(2-carbamoylbenzofuran-5-yl)piperazine-1-carboxylate | HCID 11244883 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | Tert-butyl 4-(2-cyano-1-benzofuran-5-yl)piperazine-1-carboxylate | HCID 67154775 | — |
Reaktionsschritte
The tert-butyl 4-[2-(aminocarbonyl)-1-benzofuran-5-yl]piperazine-1-carboxylate (85 mg, 0.246 mmol) was dissolved in 5 mL of DCM and cooled to 0° C. under nitrogen. Triethylamine (0.075 mL, 0.541 mmol) was added, followed by trifluoroacetic anhydride (0.038 mL, 0.271 mmol). The reaction was stirred for 1 hour, then was diluted with additional 20 mL of DCM and washed with water (2×40 mL). The organic layers were combined, dried over sodium sulfate, filtered and concentrated to afford tert-butyl 4-(2-cyano-1-benzofuran-5-yl)piperazine-1-carboxylate.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08273737B2 |
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| Quelldatensatz | uspto-grants-2012_09 |
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| ORD ID | ord-e1c2fb2a86d248208d1585cf22ab9967 |
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| Quellennotiz | uspto-grants-2012_09 |
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